721172000: Hypomagnesemia co-occurrent with normocalciuria (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hypomagnesemia co-occurrent with normocalciuria
• \Metabolic disease\Metabolic disorder of transport\Primary hypomagnesemia\Hypomagnesemia co-occurrent with normocalciuria
• \Metabolic disease\Disorder of fluid AND/OR electrolyte\Disorder of electrolytes\Magnesium disorder\Hypomagnesemia\Primary hypomagnesemia\Hypomagnesemia co-occurrent with normocalciuria

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3324518018	Hypomagnesemia co-occurrent with normocalciuria (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3324519014	Hypomagnesemia co-occurrent with normocalciuria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3324520015	Hypomagnesaemia with normocalciuria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3324521016	Hypomagnesemia with normocalciuria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3780924012	Hypomagnesaemia co-occurrent with normocalciuria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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